A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065122



Internal ID20632162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:91324907..91329992hg38UCSC Ensembl
chr1:91790464..91795549hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg385086
hg195086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318482
Supporting Variants
Samples
Known GenesHFM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065122
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer